Canonical Allele Identifier: PA2580264261
Gene: FLG HGNC NCBI

Linked Data

ClinVar Variation Id: 2366009
ClinVar RCV Id: RCV002987414

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002007.1:p.Arg879Met
CA1107069
NM_002016.2:c.2636G>T